Metabolic interventions: A new insight into the cancer immunotherapy

被引:9
|
作者
Yu, Tao [1 ]
Dong, Tianhan [2 ]
Eyvani, Haniyeh [1 ]
Fang, Yuanzhang [1 ]
Wang, Xiyu [3 ]
Zhang, Xinna [1 ,4 ]
Lu, Xiongbin [1 ,4 ,5 ]
机构
[1] Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Med Scientist Training Program, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Melvin & Bren Simon Canc Ctr, Indianapolis, IN 46202 USA
[5] Indiana Univ Sch Med, Ctr Computat Biol & Bioinformat, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
Metabolic reprogramming; Nutrients competing; Tumor microenvironment; Tumor-infiltrating lymphocytes; Immunometabolism; FATTY-ACID-METABOLISM; CELL LUNG-CANCER; GLUTAMINASE INHIBITOR CB-839; PROTON PUMP INHIBITORS; ANTITUMOR-ACTIVITY; LACTIC-ACID; TUMOR MICROENVIRONMENT; GLUCOSE-METABOLISM; AEROBIC GLYCOLYSIS; ENERGY-METABOLISM;
D O I
10.1016/j.abb.2020.108659
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metabolic reprogramming confers cancer cells plasticity and viability under harsh conditions. Such active alterations lead to cell metabolic dependency, which can be exploited as an attractive target in development of effective antitumor therapies. Similar to cancer cells, activated T cells also execute global metabolic reprogramming for their proliferation and effector functions when recruited to the tumor microenvironment (TME). However, the high metabolic activity of rapidly proliferating cancer cells can compete for nutrients with immune cells in the TME, and consequently, suppressing their anti-tumor functions. Thus, therapeutic strategies could aim to restore T cell metabolism and anti-tumor responses in the TME by targeting the metabolic dependence of cancer cells. In this review, we highlight current research progress on metabolic reprogramming and the interplay between cancer cells and immune cells. We also discuss potential therapeutic intervention strategies for targeting metabolic pathways to improve cancer immunotherapy efficacy.
引用
收藏
页数:16
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